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In some cases, the CFTR protein is prevented entirely to take place at all and in some cases, CFTR protein does produce and get its way into the cell membrane but cannot operate properly.
One way of treatment method is to supply a different class of chloride channel to compensate for the loss of the CFTR chloride channel. Gene therapy could be a better solution in future in which a normal copy of the CFTR gene to the cells is delivered. In this way, direct synthesis of the normal CFTR protein will be possible to treat the biochemical abnormality leading to cystic fibrosis. Introducing healthy gene will take over all functions of the CFTR protein that are necessary including those which are yet not known. And the best way of gene therapy is to exploit the ability of viruses bringing their DNA to enter into cells. Adenoviruses are suitable for this purpose due to their natural tendency to infect human
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(Biochemistry - Cystic Fibrosis Essay Example | Topics and Well Written Essays - 250 Words)
“Biochemistry - Cystic Fibrosis Essay Example | Topics and Well Written Essays - 250 Words”, n.d. https://studentshare.org/miscellaneous/1664532-biochemistry-cystic-fibrosis.
These diseases are inherited since the genetic information is precisely copied before being passed on to the offspring from the parents. When a single altered gene is inherited, it is called autosomal dominant. For instance, Huntington's disease is a disease resulting from the inheritance of a single mutated gene.
1. Role in mucus production O-glycans can be found attached to mucins through an O-glycosidic bond to the oxygen of the hydroxyl group of serine, threonine or hydroxyl-lysine residues of the protein. Since it is typical for mucin-related proteins to have tandem repeats rich with Ser/Thr residues, these amino acids become teeming with O-glycans.
With a tremendous advance in medical and laboratory analysis during the past years, researchers have been able to find information from the measurement of enzymes. In most cases, a clinical diagnosis, based on signs and symptoms, is complemented by laboratory tests, which bring answers to clinical questions and decisions.
The effects of CF are devastating, but life expectancy in the last 70 years since it was first written about has increased from almost certain death in infancy to 37 years of age. The following paper discusses the nature of CF through a brief
The disease usually affects the liver, intestines, pancreas, lungs and sex organs (Rosaler 2007).
Mucus provides a lining cavity to the organs, and individual suffering from the disease has mucus that is sticky
The specific health problem of this community the prevalence of Cystic Fibrosis which has not been given much attention by most health care givers, yet it disrupts the daily activities of the community. The most affected groups in this community are the expectant mothers and the unborn babies who are at risk inheriting the genes.
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